Simultaneous Profiling of Chromatin-Associated RNA at Targeted DNA Loci and RNA-RNA Interactions through TaDRIM-Seq
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报告开始：2024年11月01日 17:10 （Asia/Shanghai）
报告时间：20min
所在会议：[S3] 分会场三：三维基因组学技术（新技术、分析工具与AI） » [S3-1] 分会场三：三维基因组学技术（新技术、分析工具与AI）
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摘要
Eukaryotic genomes are extensively transcribed into various types of RNAs, many of which are physically associated with chromatin in cisat their transcription sites or in transto other genomic loci. Emerging roles have been uncovered for these chromatin-associated RNAs (caRNAs) in gene regulation and genome organization, yet they remain challenging to interrogate. Here, we present TaDRIM-seq, a technique employing Protein G (PG)-Tn5-targeted DNA elements and in situ proximity ligation to concurrently probe caRNAs across diverse genomic regions as well as global RNA-RNA interactions within intact nuclei.Notably, this approach diminishes required cell inputs, minimizes hands-on time compared to established methodologies, and is compatible in both mammalian cells and plants. Using this technique, we identified extensive caRNAs at DNA anchor regions associated with chromatin loops and revealed diurnal variation in RNA-DNA and RNA-RNA connectivity networks within rice.
Eukaryotic genomes are extensively transcribed into various types of RNAs, many of which are physically associated with chromatin in cisat their transcription sites or in transto other genomic loci. Emerging roles have been uncovered for these chromatin-associated RNAs (caRNAs) in gene regulation and genome organization, yet they remain challenging to interrogate. Here, we present TaDRIM-seq, a technique employing Protein G (PG)-Tn5-targeted DNA elements and in situ proximity ligation to concurrently probe caRNAs across diverse genomic regions as well as global RNA-RNA interactions within intact nuclei.Notably, this approach diminishes required cell inputs, minimizes hands-on time compared to established methodologies, and is compatible in both mammalian cells and plants. Using this technique, we identified extensive caRNAs at DNA anchor regions associated with chromatin loops and revealed diurnal variation in RNA-DNA and RNA-RNA connectivity networks within rice.
Eukaryotic genomes are extensively transcribed into various types of RNAs, many of which are physically associated with chromatin in cisat their transcription sites or in transto other genomic loci. Emerging roles have been uncovered for these chromatin-associated RNAs (caRNAs) in gene regulation and genome organization, yet they remain challenging to interrogate. Here, we present TaDRIM-seq, a technique employing Protein G (PG)-Tn5-targeted DNA elements and in situ proximity ligation to concurrently probe caRNAs across diverse genomic regions as well as global RNA-RNA interactions within intact nuclei.Notably, this approach diminishes required cell inputs, minimizes hands-on time compared to established methodologies, and is compatible in both mammalian cells and plants. Using this technique, we identified extensive caRNAs at DNA anchor regions associated with chromatin loops and revealed diurnal variation in RNA-DNA and RNA-RNA connectivity networks within rice.
关键字
TaDRIM-seq, Chromatin-Associated RNA, RNA-RNA interactions，DNA Elements
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